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A Network Medicine Approach for Drug Repurposing in Duchenne Muscular Dystrophy
Duchenne muscular dystrophy (DMD) is a progressive hereditary muscular disease caused by a lack of dystrophin, leading to membrane instability, cell damage, and inflammatory response. However, gene-editing alone is not enough to restore the healthy phenotype and additional treatments are required. I...
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| Publicado no: | Genes (Basel) |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8069953/ https://ncbi.nlm.nih.gov/pubmed/33918694 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes12040543 |
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